HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 8-(1-bromoethyl)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Quinoline, 8-ethyl- | HCID 88185 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 8-(1-bromoethyl)quinoline | HCID 12644813 | 78% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A solution of (12) (3.0 g, 19.1 mmol) in carbon tetrachloride (30 mL) was added NBS (5.10 g, 28.6 mmol), and benzoyl peroxide (0.12 g, 0.48 mmol). The mixture was heated at 100° C. for 3 hours. The reaction was cooled to room temperature. The mixture was filtered through filter paper, and washed with ethyl acetate. The filtrate was adsorbed into silica gel. The mixture was purified by chromatography on silica gel with 5 to 15% ethyl acetate in hexane to give 8-(1-bromoethyl)quinoline (13) (3.5 g, 14.8 mmol, 78% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119807B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-a74609774a004dd1a250f30eb5ffdf58 |
| Source note | uspto-grants-2012_02 |